Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis

Like many bacteria, Enterococcus faecalis encodes a number of adhesins involved in colonization or infection of different niches. Two well-studied E. faecalis adhesins, aggregation substance (AS) and endocarditis- and biofilm-associated pili (Ebp), both contribute to biofilm formation on abiotic sur...

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Main Authors: Afonina, Irina, Lim, Xin Ni, Tan, Rosalind, Kline, Kimberly A.
Other Authors: Brun, Yves V.
Format: Article
Language:English
Published: 2018
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Online Access:https://hdl.handle.net/10356/89710
http://hdl.handle.net/10220/47123
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-897102020-09-21T11:31:59Z Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis Afonina, Irina Lim, Xin Ni Tan, Rosalind Kline, Kimberly A. Brun, Yves V. School of Social Sciences Singapore Centre for Environmental Life Sciences Engineering DRNTU::Science::Biological sciences Horizontal Gene Transfer Enterococcus faecalis Like many bacteria, Enterococcus faecalis encodes a number of adhesins involved in colonization or infection of different niches. Two well-studied E. faecalis adhesins, aggregation substance (AS) and endocarditis- and biofilm-associated pili (Ebp), both contribute to biofilm formation on abiotic surfaces and in endocarditis, suggesting that they may be expressed at the same time. Because different regulatory pathways have been reported for AS and Ebp, here, we examined if they are coexpressed on the same cells and what is the functional impact of coexpression on individual cells and within a population. We found that while Ebp are only expressed on a subset of cells, when Ebp and AS are expressed on the same cells, pili interfere with AS-mediated clumping and impede AS-mediated conjugative plasmid transfer during planktonic growth. However, when the population density increases, horizontal gene transfer rates normalize and are no longer affected by pilus expression. Instead, at higher cell densities during biofilm formation, Ebp and AS differentially contribute to biofilm development and structure, synergizing to promote maximal biofilm formation. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Published version 2018-12-20T06:19:47Z 2019-12-06T17:31:43Z 2018-12-20T06:19:47Z 2019-12-06T17:31:43Z 2018 Journal Article Afonina, I., Lim, X. N., Tan, R., & Kline, K. A. (2018). Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis. Journal of Bacteriology, 200(24), e00361-18-. doi: 10.1128/JB.00361-18 0021-9193 https://hdl.handle.net/10356/89710 http://hdl.handle.net/10220/47123 10.1128/JB.00361-18 en Journal of Bacteriology © 2018 Afonina et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. 11 p. application/pdf
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences
Horizontal Gene Transfer
Enterococcus faecalis
spellingShingle DRNTU::Science::Biological sciences
Horizontal Gene Transfer
Enterococcus faecalis
Afonina, Irina
Lim, Xin Ni
Tan, Rosalind
Kline, Kimberly A.
Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis
description Like many bacteria, Enterococcus faecalis encodes a number of adhesins involved in colonization or infection of different niches. Two well-studied E. faecalis adhesins, aggregation substance (AS) and endocarditis- and biofilm-associated pili (Ebp), both contribute to biofilm formation on abiotic surfaces and in endocarditis, suggesting that they may be expressed at the same time. Because different regulatory pathways have been reported for AS and Ebp, here, we examined if they are coexpressed on the same cells and what is the functional impact of coexpression on individual cells and within a population. We found that while Ebp are only expressed on a subset of cells, when Ebp and AS are expressed on the same cells, pili interfere with AS-mediated clumping and impede AS-mediated conjugative plasmid transfer during planktonic growth. However, when the population density increases, horizontal gene transfer rates normalize and are no longer affected by pilus expression. Instead, at higher cell densities during biofilm formation, Ebp and AS differentially contribute to biofilm development and structure, synergizing to promote maximal biofilm formation.
author2 Brun, Yves V.
author_facet Brun, Yves V.
Afonina, Irina
Lim, Xin Ni
Tan, Rosalind
Kline, Kimberly A.
format Article
author Afonina, Irina
Lim, Xin Ni
Tan, Rosalind
Kline, Kimberly A.
author_sort Afonina, Irina
title Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis
title_short Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis
title_full Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis
title_fullStr Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis
title_full_unstemmed Planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in Enterococcus faecalis
title_sort planktonic interference and biofilm alliance between aggregation substance and endocarditis- and biofilm-associated pili in enterococcus faecalis
publishDate 2018
url https://hdl.handle.net/10356/89710
http://hdl.handle.net/10220/47123
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